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Computer System Validation Csv Pharmaceutical Jobs in Springfield, TN

Develop codes, labels and other predefined formats for pharmacy computer entry * You will assist as ... You will retrieve and interpret medication orders; perform complex procedures and pharmaceutical ...

Develop codes, labels and other predefined formats for pharmacy computer entry * You will assist as ... You will retrieve and interpret medication orders; perform complex procedures and pharmaceutical ...

Develop codes, labels and other predefined formats for pharmacy computer entry * You will assist as ... You will retrieve and interpret medication orders; perform complex procedures and pharmaceutical ...

Pharmacy Technician

Nashville, TN · On-site

$17 - $20.50/hr

... computer system. * Assist in managing refill requests, prior authorizations, and medication transfers between pharmacies. * Quality Assurance: * Perform quality assurance checks on medication ...

New

Pharmacy Manager

Nashville, TN · On-site

$61.75 - $72.50/hr

Orders products using a computer system. Coordinates proper maintenance and repairs for machinery ... Acts as Pharmacist-In-Charge, as point of contact for regulatory, legal, third party insurance ...

Pharmacy Technician

Nashville, TN · On-site

$17 - $20.50/hr

... computer system. * Assist in managing refill requests, prior authorizations, and medication transfers between pharmacies. * Quality Assurance: * Perform quality assurance checks on medication ...

New

Pharmacy Manager

Mount Juliet, TN · On-site

$61.50 - $72.25/hr

Orders products using a computer system. Coordinates proper maintenance and repairs for machinery ... Acts as Pharmacist-In-Charge, as point of contact for regulatory, legal, third party insurance ...

Showing results 41-60

Computer System Validation Csv Pharmaceutical information

See Springfield, TN salary details

$9

$51

$81

How much do computer system validation csv pharmaceutical jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for computer system validation csv pharmaceutical in Springfield, TN is $51.30, according to ZipRecruiter salary data. Most workers in this role earn between $39.52 and $60.82 per hour, depending on experience, location, and employer.

What is the difference between Computer System Validation Csv Pharmaceutical vs Quality Assurance Specialist?

AspectComputer System Validation Csv PharmaceuticalQuality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, Validation certificationsGxP, ISO, QA certifications
Work EnvironmentPharmaceutical manufacturing, regulated labsQuality departments across industries, including pharma
Employer & IndustryPharmaceutical companies, biotech firmsPharma, biotech, healthcare organizations
Primary FocusEnsuring computer systems meet validation and compliance standardsMaintaining quality standards and process improvements

Computer System Validation Csv Pharmaceutical specialists focus on validating computer systems to ensure compliance with industry regulations, while Quality Assurance Specialists oversee overall quality processes. Both roles require GxP knowledge and are vital in pharmaceutical environments, but their core responsibilities differ in scope and focus.

What are common challenges faced by computer system validation (CSV) professionals in the pharmaceutical industry?

CSV professionals in the pharmaceutical industry often encounter challenges such as keeping up with evolving regulatory requirements, managing documentation for audits, and ensuring thorough validation of complex systems within tight project timelines. Collaboration with cross-functional teams, such as IT, quality assurance, and manufacturing, is essential to address technical and compliance issues. Additionally, balancing the need for robust validation with operational efficiency requires strong communication and project management skills.

What are the key skills and qualifications needed to thrive as a computer system validation (CSV) professional in the pharmaceutical industry?

To thrive as a Computer System Validation (CSV) professional in pharmaceuticals, you need a strong background in life sciences or engineering, knowledge of regulatory standards (such as FDA 21 CFR Part 11), and experience with validation protocols. Familiarity with validation lifecycle management tools, quality management systems (QMS), and industry guidelines like GAMP 5 is typically required, along with certifications such as ISPE or PMP being advantageous. Outstanding attention to detail, analytical thinking, and strong communication skills help ensure compliance and effective coordination with cross-functional teams. These competencies are vital for maintaining regulatory compliance, data integrity, and patient safety in pharmaceutical operations.

What is computer system validation (CSV) in the pharmaceutical industry?

Computer System Validation (CSV) in the pharmaceutical industry is a process used to ensure that computerized systems used in drug manufacturing and related processes work as intended and comply with regulatory standards, such as FDA 21 CFR Part 11. CSV involves planning, testing, documenting, and maintaining systems to guarantee the accuracy, reliability, and integrity of data. This is critical for patient safety and product quality, as well as for meeting legal and regulatory requirements. The process typically includes risk assessment, validation planning, protocol execution, and ongoing monitoring of system performance.

What cities near Springfield, TN are hiring for Computer System Validation Csv Pharmaceutical jobs?

Cities near Springfield, TN with the most Computer System Validation Csv Pharmaceutical job openings:

Infographic showing various Computer System Validation Csv Pharmaceutical job openings in Springfield, TN as of August 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $106,699 per year, or $51.3 per hour.

Full-time

Posted 10 days ago


Job description

It’s More Than a Career, It’s a Mission.


Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission


People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As the Research Pharmacist you will oversee the investigational pharmacy operations and the pharmacy technical staff to support our institution’s growing involvement in clinical research activities. This service will provide support to industry-sponsored and investigator-initiated trials for multiple research sites in the outpatient setting. The investigational drug research pharmacist will interact with investigators, study sponsors, research colleagues and other healthcare providers.

  • You will create, monitor, document, and follow departmental SOPs, corporate guidelines and conventions providing quality and accurate investigational pharmacy services

  • You will develop, monitor and maintain step-by-step procedures (e.g., kits) for preparation, dispensing and distribution of investigational and study drugs. Develop codes, labels and other predefined formats for pharmacy computer entry

  • You will assist as needed in preparing reports for company management and regulatory agencies.

  • You will evaluate study protocols to determine appropriate resources and materials needed to satisfy study requirements

  • You will retrieve and interpret medication orders; perform complex procedures and pharmaceutical calculations, taking into account research protocol, patient and drug characteristics

  • You will perform specialized and advanced procedures specific to assigned pharmacy area; label, fill and provide delivery oversight of investigational drugs to appropriate patient care locations

  • You will be responsible for establishing and continually improving the shipment and delivery of investigational pharmaceutical care to patients within areas of direct responsibility and assisting others in the department with the same

  • You will have an ongoing review of study protocols to determine appropriate pharmaceutical materials and professional services required to satisfy the study description

  • You will establish and maintain accurate and easily retrievable recordkeeping systems for protocols, study subjects, tracking logs, schedules, drug accountability records, and systems

  • You will ensure site staff, Study Chairs, and members of the Consortium department understand the investigational drug maintenance, dispense and distribution process

  • You will collaborate with Study Chairs and relevant staff to provide investigational drug trending and status reporting as needed for assigned clinical trials

  • You will maintain positive and cooperative relationship in day-to-day interactions and communications

  • You will manage performance and development of Pharmacy staff members, budget and goals

  • You will oversee the activities of assigned pharmacy technicians engaged in the preparation, labeling and delivery of investigational drugs and other pharmaceutical supplies in accordance with physicians' orders; ensure accuracy and compliance with federal, state and local laws and regulations pertaining to the dispensing of drugs and the maintenance of required records

You should have for this position:

  • A Doctorate Degree

  • Licensed Pharmacist

  • Knowledge of FDA guidelines and GCP is required

  • Minimum of one year of Chemotherapy Admixture experience

  • Must be able to read, understand, and comply with research protocols

  • Must be able to perform duties commensurate with dispensing medications with narrow therapeutic indices

  • A Minimum of one year of Clinical research experience preferred

About Sarah Cannon Research Institute


Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.
We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.
As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.


McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.